Evidence map›Paper›PMID 42518973›Full record

ArticleClinical neurophysiology practice2026

Sex-independent visual evoked potential complexity.

Łukasz Lisowski, Łukasz Łabieniec, Jolanta Lisowska, Andrzej Andrejczuk, Dominik Zalewski, Joanna Konopińska

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Article in Clinical neurophysiology practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Łukasz LisowskiDepartment of Ophthalmology, Medical University of Bialystok, Poland.
Łukasz ŁabieniecFaculty of Physics, University of Bialystok, Poland.
Jolanta LisowskaIndividual Medical Practice, Bialystok, Poland.
Andrzej AndrejczukFaculty of Physics, University of Bialystok, Poland.
Dominik ZalewskiLens Center for Eye Diagnostics and Microsurgery, Poland.
Joanna KonopińskaDepartment of Ophthalmology, Medical University of Bialystok, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Visual evoked potentials (VEPs) provide a non-invasive measure of visual pathway function, traditional analyses focusing on peak latency and amplitude may overlook the dynamic complexity of cortical processing. This study examined whether VEP signal complexity differs between sexes using a non-linear fractal approach based on the correlation dimension (D₂). Methods: Eighty-eight healthy adults (39 females, 49 males; mean age 37 years) underwent pattern-reversal VEP testing for each eye using two checkerboard field sizes (0.808° and 0.258°), preferentially engaging magnocellular and parvocellular pathways. The complexity of averaged VEPs was quantified using the Grassberger-Procaccia algorithm with optimised embedding parameters. Sex and eye effects were analysed separately for each stimulus condition. Results: No significant main effects or interactions of sex or eye were observed for either checkerboard size. Estimated D₂ values ranged from 3.3 to 3.6 across conditions. Although females showed numerically higher P100 amplitudes, particularly for small-checkerboard stimulation, and a subtle tendency toward longer response latencies for left-eye stimulation, these differences were not reflected in D₂. Conclusions: The fractal dimensionality of early visual cortical responses is stable across sex, eye, and stimulus parameters. Significance: Correlation dimension (D₂) analysis can be applied to averaged visual evoked potential (VEP) data from healthy adults without stratifying participants by sex.

Indexed as

Correlation dimensionElectrophysiologyFractal dimensionNeural complexitySex differenceVisual evoked potential

Identifiers

PMID42518973
PMCPMC13383331

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.